In this second of a two-part review encompassing random, combinatorial methods for soluble protein ‘domain hunting’, we focus upon the expression screening from DNA fragment libraries. Given a library of domain length-encoding DNA fragments assembled in expression vectors, it is necessary to devise reliable means to screen the sample DNA fragment population to find those that express stable, soluble target protein fragments, suitable for the required downstream aims. This review summarizes a variety of alternative strategies that have been employed to identify such stable truncates of full-length proteins. In addition, we review measures that can determine the quality of the expressed protein, the likely reliability of these measures, and t...
Directed molecular evolution and combinatorial methodologies are playing an increasingly important r...
Producing soluble proteins in Escherichia coli is still a major bottleneck for structural proteomics...
Exploring the function and 3D space of large multidomain protein targets often requires sophisticate...
In this second of a two-part review encompassing random, combinatorial methods for soluble protein '...
In addressing a new drug discovery target, the generation of tractable protein substrates for functi...
In addressing a new drug discovery target, the generation of tractable protein substrates for functi...
Exploitation of potential new targets for drug and vaccine development has an absolute requirement f...
Exploitation of potential new targets for drug and vaccine development has an absolute requirement f...
We describe here a systematic approach to the identification of human proteins and protein fragments...
We describe here a systematic approach to the identification of human proteins and protein fragments...
Structural biology studies typically require large quantities of pure, soluble protein. Currently th...
We describe here a systematic approach to the identification of human proteins and protein fragments...
PCR-based amplification of annotated genes has allowed construction of expression clones at genome-s...
Structural biology studies typically require large quantities of pure, soluble protein. Currently th...
Producing soluble proteins in Escherichia coli is still a major bottleneck for structural proteomics...
Directed molecular evolution and combinatorial methodologies are playing an increasingly important r...
Producing soluble proteins in Escherichia coli is still a major bottleneck for structural proteomics...
Exploring the function and 3D space of large multidomain protein targets often requires sophisticate...
In this second of a two-part review encompassing random, combinatorial methods for soluble protein '...
In addressing a new drug discovery target, the generation of tractable protein substrates for functi...
In addressing a new drug discovery target, the generation of tractable protein substrates for functi...
Exploitation of potential new targets for drug and vaccine development has an absolute requirement f...
Exploitation of potential new targets for drug and vaccine development has an absolute requirement f...
We describe here a systematic approach to the identification of human proteins and protein fragments...
We describe here a systematic approach to the identification of human proteins and protein fragments...
Structural biology studies typically require large quantities of pure, soluble protein. Currently th...
We describe here a systematic approach to the identification of human proteins and protein fragments...
PCR-based amplification of annotated genes has allowed construction of expression clones at genome-s...
Structural biology studies typically require large quantities of pure, soluble protein. Currently th...
Producing soluble proteins in Escherichia coli is still a major bottleneck for structural proteomics...
Directed molecular evolution and combinatorial methodologies are playing an increasingly important r...
Producing soluble proteins in Escherichia coli is still a major bottleneck for structural proteomics...
Exploring the function and 3D space of large multidomain protein targets often requires sophisticate...